You can also attach this data to the Ensembl Browser as explained in this tutorial page. You will have your data in a format like 'chr start end individual' (i.e. BED format) and you can compare it to our gene annotation, our variation data (variants annotated according to consequence terms), and regulation data from ENCODE, Blueprint and Roadmap projects (for annotation of enhancer promoter, CTCF, etc). We also include the CNVs from 1000 Genomes and structural variants from DECIPHER (see the region where PRR29 is anntoated). Once you attach your data, you also have the option to share that visualisation with your colleagues and collaborators. You just send them the URL we generate and they will see your data against our annotation.